Canonical Allele Identifier: PA2825021511
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 579159

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.His1738Asp
CA16032725
NM_000038.6:c.5212C>G